Related Experiment Video For Multiple endocrine neoplasia type 1
Updated: Dec 6, 2025

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Multiple endocrine neoplasia type 1 (MEN1) presenting with renal stones: Case report and review
Mohamed N Ibrahim1, James Liem1, Ahmed ElKady1
1Department of Diagnostic Radiology, Rotherham General Hospital, Moorgate Road, Rotherham, South Yorkshire S60 2UG, United Kingdom.
Abstract:
Multiple endocrine neoplasia type 1 (MEN1) is a complex, autosomal dominant inherited syndrome characterized by 3 different tumors (parathyroid, anterior pituitary, and pancreatic islet). The diagnosis is defined clinically by the presence of 2 or more primary tumors. We report the case of a 35 years old patient who presented with recurrent renal stones and imaging findings for MEN1. Computed tomography pancreas revealed a mass in the tail which was confirmed by magnetic resonance imaging. Ultrasound of her neck showed a mass on the left side and MIBI scan diagnosed a parathyroid adenoma which was later pathologically confirmed.
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